Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17817449
rs17817449
FTO
21 0.716 0.560 16 53779455 intron variant T/A;G snv 0.720 1.000 7 2013 2017
dbSNP: rs11075995
rs11075995
FTO
5 0.882 0.080 16 53821379 intron variant A/T snv 0.77 0.720 1.000 5 2013 2017
dbSNP: rs56077980
rs56077980
FTO
1 1.000 0.080 16 54107654 intron variant -/T delins 0.26 0.700 1.000 1 2017 2017
dbSNP: rs62048402
rs62048402
FTO
3 0.882 0.200 16 53769311 intron variant G/A snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.040 0.750 4 2013 2017
dbSNP: rs1477196
rs1477196
FTO
7 0.851 0.200 16 53774346 intron variant A/G snv 0.71 0.030 1.000 3 2011 2015
dbSNP: rs1121980
rs1121980
FTO
18 0.807 0.240 16 53775335 intron variant G/A;C snv 0.020 0.500 2 2013 2015
dbSNP: rs16953002
rs16953002
FTO
5 0.882 0.080 16 54080912 intron variant G/A snv 0.19 0.010 1.000 1 2015 2015